.
Logo
  • PRODUCTS
  • TECHNOLOGY
  • COMPANY
  • CAREERS
  • Support
  • COMMUNITY
  • Sign in
  1. Support
  2. Q&A
Q&A NEW CONTACT SUPPORT
  1. 10X Genomics
  2. General Single Cell RNA-seq
  3. GEM Generation & Barcoding

GEM Generation & Barcoding

  • How should I take photographs to document clogs and wetting failures?
  • How can I test whether my cells can be partitioned into GEMs?
  • Is it possible to capture microRNAs in the Gene Expression assays?
  • Can you run Single Cell 5' and 3' samples on the same Single Cell A Chip?
  • What is a template switch oligo (TSO)?
  • What is the maximum number of cells that can be profiled?
  • Recommended plastics for GEM-RT reaction
  • Is a heat sealer necessary to seal the plate after GEM recovery?
  • What are the properties of the Gel Bead-in-Emulsion (GEMs)?
  • Should I proceed if there is a sample clog?
  • How often do multiple Gel Beads end up in a partition?
  • Can GEMs be stored after isothermal incubation?
  • Can GEMs be stored after the partitioning of single cells?
  • What is a wetting failure and how can they be recognized?
footer-logo

Biology at True Resolution

About
  • Solutions
  • Technology
  • Company
  • Careers
  • Support
  • Community
  • Contact Us
Legal Notices
  • Privacy Policy
  • Terms of Use
  • Email Preferences
  • Other Legal Notices
Resources
  • Publications
  • Applications
  • Videos
Headquarters
  • +1 925 401 7300
  • +1 800 709 1208
  • info@10xgenomics.com
Social
©2018 10x Genomics. All Rights Reserved.
Sign up for product and event updates